(Re) Setting 100% mineral Powder Light Broad Spectrum SPF 35

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
(Re) Setting 100% mineral Powder Light Broad Spectrum SPF 35
Generic name
ZINC OXIDE
Manufacturer
Supergoop, LLC
Product type
HUMAN OTC DRUG
SPL set ID
aed5a7ef-5cf2-6738-e053-2a95a90aa7f7
SPL ID
47f8a103-8ed0-6eff-e063-6394a90a1aaf
Version
6
Effective date
2026-01-09
Source export date
2026-10-27
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:37:37
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.